24171-85-5

Basic information

• Product Name: Benzoic acid, 4-(hydroxyamino)-, ethyl ester
• Synonyms: 4-hydroxyamino-benzoic acid ethylester;Benzoic acid,4-(hydroxyamino)-,ethyl ester;(4-carbethoxyphenyl)hydroxylamine;p-hydroxyaminobenzoic acid etyl ester;4-CO2EtC6H4-NHOH;ethyl 4-(hydroxylamino)benzoate;ethyl p-(hydroxylamino)benzoate
• CAS NO: 24171-85-5
• Molecular Formula: C9H11NO3
• Molecular Weight: 181.191
• Mol File: 24171-85-5.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-(hydroxyamino)-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-(hydroxyamino)-, ethyl ester(24171-85-5)
• EPA Substance Registry System: Benzoic acid, 4-(hydroxyamino)-, ethyl ester(24171-85-5)

Safety Data

• Hazardous Substances Data: 24171-85-5(Hazardous Substances Data)

Upstream product

• 99-77-4 ethyl 4-nitrobenzoate 
• 94-09-7 p-aminoethylbenzoate 
• 1303610-40-3 4-CO₂EtC₆H₄-N(Teoc)OTBS 

Downstream Products

• 94-09-7 p-aminoethylbenzoate 
• 94664-79-6 N-(4-ethoxycarbonylphenyl)-α-phenylnitrone 
• 948308-96-1 N-(4-ethoxycarbonylphenyl)-α-(3-chlorophenyl)nitrone 
• 93749-88-3 α-(4-(diethylamino)phenyl)-N-(4-carbethoxyphenyl)nitrone 
• 94664-79-6 N-(4-carboethoxyphenyl)-α-phenylnitrone 
• 21000-76-0 ethyl 2-methyl-3-phenethyl-1H-indole-5-carboxylate 
• 1416899-29-0 α-(4-methoxycarbonylphenyl)-N-(4-ethoxycarbonylphenyl)nitrone 
• 1204476-69-6 α-(4-dimethylaminostyryl)-N-(4-carbethoxyphenyl)nitrone 
• 1134370-18-5 2,5-bis(N-(4-ethoxycarbonylphenyl)imino-N-oxide)thiophene 

Relevant articles and documents

Ultrasonically activated reduction of substituted nitrobenzenes to corresponding N-arylhydroxylamines

Arylhydroxylamines can be obtained by reduction of the corresponding nitroaromatic compounds. We report here an efficient preparation of arylhydroxylamines by a controlled reduction of nitro compounds using zinc metal and ammonium chloride under ultrasonic activation in very short reaction times.

HOLOGRAPHIC RECORDING MEDIUM

Disclosed herein are novel nitrone compounds, holographic recording media that include the nitrone compound(s) and a polymer binder, a method of manufacturing a holographic recording medium where the nitrone compound, as a photochromic dye, is mixed with

Synthesis of N-arylhydroxylamines by Pd-catalyzed coupling

Pd-catalyzed coupling of aryl halides with TeocNHOTBS, followed by treatment of the products with TBAF, provides effective access to a wide range of N-arylhydroxylamines by a route that produces stable doubly-protected intermediates and allows the protective groups to be removed under mild conditions that do not cause extensive degradation of the final product.